nsv5013690
- Organism: Homo sapiens
- Study:nstd200 (Abel et al. 2020)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:10,209
- Publication(s):Abel et al. 2020
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 137 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 135 SVs from 21 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv5013690 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000017.11 | Chr17 | 40,127,847 (-23, +23) | 40,138,055 (-23, +23) | ||
| nsv5013690 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000017.10 | Chr17 | 38,284,100 (-23, +23) | 38,294,308 (-23, +23) |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv16574437 | duplication | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv16574437 | Submitted genomic | NC_000017.11:g.(40 127824_40127870)_( 40138032_40138078) dup | GRCh38 (hg38) | NC_000017.11 | Chr17 | 40,127,847 (-23, +23) | 40,138,055 (-23, +23) | ||
| nssv16574437 | Remapped | Perfect | NC_000017.10:g.(38 284077_38284123)_( 38294285_38294331) dup | GRCh37.p13 | First Pass | NC_000017.10 | Chr17 | 38,284,100 (-23, +23) | 38,294,308 (-23, +23) |
No validation data were submitted for this variant
No clinical assertion data were submitted for this variant
Genotype Information
| Variant Call ID | Allele Frequency (AF) | Allele Count (AC) | Allele Number (AN) |
|---|---|---|---|
| nssv16574437 | <0.001 | 2 | 29246 |